Central Venous Catheter Conforming to IS 10555 (Part 3)
N/a
BHOPAL, MADHYA PRADESH
Progress
Quantity
6000
Bid Type
Two Packet Bid
Central Health Service, Ministry Of Health And Family Welfare invites bids for the procurement of a Central Venous Catheter conforming to IS 10555 (Part 3), including related accessories and packing. The scope is strictly supply of goods with an EMD of ₹78,000. The tender emphasizes regulatory compliance (MDR 2017) and required licenses under the Drugs and Cosmetics Act, with an additional focus on Make in India authorization and OEM turnover prerequisites. Location details are not disclosed in the summary, but the procurement fits the government health equipment category for centralized health programs. A key differentiator is the mandatory compliance ecosystem (MDR, IS 10555, OEM turnover) and after-sales considerations for imported or domestically manufactured items. The bid targets suppliers capable of meeting stringent regulatory and certification criteria with a robust supply chain to government bodies.
Central Venous Catheter conforming to IS 10555 (Part 3)
Minimum shelf life requirement at delivery
Accessories include introducer needle, guide-wire, dilators, syringe, scalpel blade, injection cap, extension tube with clamps, sutures
Syringe size, needle sizes, guide-wire type/length, and catheter length/Fr size must be specified by bidder
MDR 2017 compliance and valid Drugs and Cosmetics Act license
EMD ₹78,000; MSME/NSIC exemption considerations
Must have MDR 2017 compliance and IS 10555 (Part 3) conformance
OEM turnover and Make in India authorization required
Payment terms not explicitly stated; bid indicates supply of goods with applicable terms per contract; anticipate standard government terms
Delivery timeline to be defined in Purchase Order; supplier should ensure minimum shelf life at delivery
Not explicitly detailed in provided terms; penalties typically apply for delayed delivery or non-compliance per contract
Bidder must supply to government/PSU or renowned private organisations with PO history
Must meet turnover criteria for bidder and OEM over last 3 years
Make in India authorization and valid medical device licensing mandatory
Tender Category
Goods
Bid To RA
No
Bid To RA Enabled
Yes
Item Category
Central Venous Catheter Conforming to IS 10555 (Part 3) (Q2)
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Main Document
CATALOG Specification
OTHER
OTHER
OTHER
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS
N/a
BHOPAL, MADHYA PRADESH
N/a
BHOPAL, MADHYA PRADESH
All India Institute Of Medical Sciences (aiims)
SOUTH DELHI, DELHI
Directorate Of Purchase And Stores
MUMBAI, MAHARASHTRA
Indian Army
JALANDHAR, PUNJAB
Tender Results
Loading results...
| Category | Specification | Requirement |
|---|---|---|
| GENERAL | Product Description | Central Venous Catheter |
| PRODUCT INFORMATION | Catheter Type | Triple Lumen |
| PRODUCT INFORMATION | Length of catheter (mm) | 160.0 |
| PRODUCT INFORMATION | Catheter size (Fr) | 7 Fr |
| PRODUCT INFORMATION | Guidewire length (in mm) | 600.0 |
| PRODUCT INFORMATION | Distal Tip | Smooth |
| ACCESSORIES | Shape of Introducer Needle | Straight |
| ACCESSORIES | Size of introducer needle | 18 G |
| ACCESSORIES | Type of guide-wire | J Tip |
| ACCESSORIES | Guide-wire size | 0.035 inch |
| ACCESSORIES | Number of Dilator | 1 |
| ACCESSORIES | Syringe Size | 5 ml |
| ACCESSORIES | Scalpel Blade Size | No. 11 |
| ACCESSORIES | Injection Cap | Yes |
| ACCESSORIES | Extension Tube with Slide Clamps | Yes |
| ACCESSORIES | Surgical Needled Suture | Yes |
| PACKING | Type of Packing | All Components Packed Together in a Transparent Pack |
| CERTIFICATIONS | Compliance to Medical Device Rules (MDR) 2017 as amended till date | Yes |
| CERTIFICATIONS | Availability of valid medical device license number for the product issued from the competent authority defined under Drugs and Cosmetic Act 1940 and Rules made there under as amended till date | Yes |
| SHELF LIFE | Minimum shelf life of the product at the time of delivery to the consignee | 3/4 th of Total Shelf Life |
Discover companies most likely to bid on this tender
GST registration certificate
Permanent Account Number (PAN) card
Experience certificates for supply to Govt/PSU/private organisations
Audited financial statements or CA certificate for turnover (last 3 years)
EMD submission proof (₹78,000) or MSME/NSIC exemption certificate
Medical device license number valid in India
MDR compliance documentation
Make in India authorization certificate
OEM authorization (for imported products) and domestic after-sales support proof
Extended Deadline
13-Jun-2026, 9:00 am
Opening Date
13-Jun-2026, 9:30 am
Key insights about DELHI tender market
Bidders must submit GST, PAN, experience certificates, financial statements, and EMD ₹78,000 (unless MSME/NSIC exempt). Provide MDR compliance, IS 10555 (Part 3) conformance, and Make in India authorization. Include OEM authorization for imported items and ensure turnover criteria are met for bidder and OEM.
Submit GST certificate, PAN card, experience certificates, audited financial statements or CA certificate, EMD proof of ₹78,000, medical device license number, MDR compliance, Make in India authorization, and OEM authorization if applicable. Ensure government/PSU purchase order exposure is demonstrated.
Products must comply with IS 10555 (Part 3), MDR 2017, and Drugs and Cosmetics Act licenses. Bid details should specify catheter length, Fr size, guidewire length, distal tip, introducer needle shape/size, and syringe/extension tube components.
The tender requires an EMD of ₹78,000 at bid submission; exemptions may apply for eligible MSME/NSIC bidders upon providing exemption certificates.
Bidders must provide a Make in India authorization certificate to demonstrate local manufacture or authorised domestic supply capability, enabling eligibility for procurement under government policies.
Bidders must show average annual turnover over the last 3 years ending 31st March; OEM must meet the same turnover criterion. If a new entity, turnover is calculated from completed years after constitution as applicable.
Imported products require a valid medical device license and an OEM/Authorized Seller with India registered office for after-sales support; submit license numbers and proof of service capability in India.
Payment terms are typically per contract; bidders should expect standard government terms—ensure clear payment milestones in the Purchase Order, including submission of compliant invoices and delivery confirmation aligned with the agreed shelf-life requirement.
All India Institute Of Medical Sciences (aiims)
📍 SOUTH DELHI, DELHI
Sree Chitra Tirunal Institute For Medical Sciences And Technology (sctimst)
📍 THIRUVANANTHAPURAM, KERALA
Indian Army
📍 JALANDHAR, PUNJAB
South Eastern Railway
Sree Chitra Tirunal Institute For Medical Sciences And Technology (sctimst)
📍 THIRUVANANTHAPURAM, KERALA
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Main Document
CATALOG Specification
OTHER
OTHER
OTHER
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS